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Shukla Shoulder S9SHLDR

FDA UDI

Class I (US FDA UDI)

by Shukla Medical

Identity

Trade Name
Shukla Shoulder S9SHLDR FDA UDI
Generic Name
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI
Device Name
Shoulder Stem Extractor Jaw, Extruded Boss Mini FDA UDI
Model / Reference
STP080 FDA UDI
Description
Shoulder Stem Extractor Jaw, Extruded Boss Mini FDA UDI

Identifiers

Primary DI / UDI-DI
B756STP0800 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic inorganic implant inserter/extractor, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic inorganic implant inserter/extractor, reusable

Shukla Shoulder S9SHLDR by Shukla Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic inorganic implant inserter/extractor, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Shukla Medical

Sources (1)

  • FDA UDI 48ebb641-8d94-426c-94ac-2fdc5b7c2c77 34 fields · synced Jun 8, 2026